Array CGH analysis of copy number variation identifies 1284 new genes variant in healthy white males: Implications for association studies of complex diseases

Human Molecular Genetics

Volumn 16, Issue 23, 2007, Pages 2783-2794

  de Smith, Adam J ^a   Tsalenko, Anya ^b   Sampas, Nick ^b   Scheffer, Alicia ^b   Yamada, N Alice ^b   Tsang, Peter ^b   Ben dor, Amir ^b   Yakhini, Zohar ^b   Ellis, Richard J ^c   Bruhn, Laurakay ^b   Laderman, Stephen ^b   Froguel, Philippe ^a,d   Blakemore, Alexandra I F ^a  

^a IMPERIAL COLLEGE LONDON   (United Kingdom)

^b AGILENT LABORATORIES   (United States)

^c NORTHWICK PARK HOSPITAL   (United Kingdom)

^d INSTITUT PASTEUR DE LILLE   (France)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CAUCASIAN; COMPARATIVE GENOMIC HYBRIDIZATION; CONTROLLED STUDY; DNA MICROARRAY; GENE CLUSTER; GENE DUPLICATION; GENE FUNCTION; GENE IDENTIFICATION; GENE LOCUS; GENE NUMBER; GENE PROBE; GENETIC ASSOCIATION; GENETIC CONSERVATION; GENETIC DATABASE; GENETIC DISORDER; GENETIC VARIABILITY; HUMAN; MALE; PHENOTYPE; PRIORITY JOURNAL;

ADULT; BASE SEQUENCE; DATABASES, NUCLEIC ACID; DNA PRIMERS; FRANCE; GENE DOSAGE; HUMANS; MALE; MIDDLE AGED; OLIGONUCLEOTIDE ARRAY SEQUENCE ANALYSIS; PHENOTYPE; VARIATION (GENETICS);

EID: 35748971743     PISSN: 09646906     EISSN: 14602083     Source Type: Journal    
DOI: 10.1093/hmg/ddm208     Document Type: Article

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